RX Cholangiogram Kit M00575320Recalls & reported problems
Boston Scientific Corporation · RX Cholangiogram Kit with Olympus Compatible Biopsy Cap · Class 2
2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 2
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
2 FDA recall records name this device's identifier, 2 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Dec 22, 2021Open, Classified
Sterility of device is compromised due to a sterile barrier breach
Z-0780-2022 · Root cause: Packaging process control · FDA record ↗
- Dec 22, 2021Open, Classified
Sterility of device is compromised due to a sterile barrier breach
Z-0781-2022 · Root cause: Packaging process control · FDA record ↗
Other Endoscopic Cholangiogram Kit devices
- RX Cholangiogram Kit M00575360Boston Scientific Corporation · Endoscopic Cholangiogram Kit2 recalls1 report
- RX Cholangiogram Kit M00575440Boston Scientific Corporation · Endoscopic Cholangiogram Kit2 recalls0 reports
- RX Cholangiogram Kit M00575480Boston Scientific Corporation · Endoscopic Cholangiogram Kit2 recalls0 reports
- RX Cholangiogram Kit M00575280Boston Scientific Corporation · Endoscopic Cholangiogram Kit2 recalls0 reports
- RX Cholangiogram Kit M00575400Boston Scientific Corporation · Endoscopic Cholangiogram Kit2 recalls0 reports
- RX Cholangiogram Kit M00575380Boston Scientific Corporation · Endoscopic Cholangiogram Kit2 recalls0 reports
- RX Cholangiogram Kit M00575240Boston Scientific Corporation · Endoscopic Cholangiogram Kit2 recalls0 reports
- Cook G26908Cook Incorporated · Endoscopic Cholangiogram Kit1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.